Table 1.
Study | Location | Outcome | No of Predictors | Age | Gender | Events (n)/total participants (n) | Duration of follow-up | Modelling method | Calibration | Discrimination (with CI) | External Validation |
Yang et al 38 | Hong Kong, China | Stroke (stroke or deaths from stroke), haemorrhagic stroke and ischaemic stroke | 4 (age, A1C, spot urine ACR and history of CHD) | Median age 57 years | Both male and female | 372/7209 | Median follow-up 5.37 years | Cox proportional hazard model | The Life Table Method. Adequate calibration, value NR. | Adjusted: AUROC=0.776 (considering follow-up time and censoring); unadjusted AUROC=0.749 (0.716 to 0.782) | No |
Kothari et al 21 | UK | Stroke (defined as a neurological deficit with symptoms or signs lasting 1 month or more) | 7 (duration of diabetes, age, sex, smoking, systolic blood pressure, total cholesterol to high-density lipoprotein cholesterol ratio and presence of atrial fibrillation) | 25 to 65 years | Both male and female | 188/4549 | Median follow-up 10.5 years | Maximum likelihood estimation using the Newton-Raphson method | NR | NR | Yes |
Wells et al 47 | USA | CHD, heart failure, stroke, mortality | 29 (different variables for different models) | 18 years of age or older | Both male and female | Stroke: 1088/26 140 | Median follow-up 501 days (Stroke model) | Competing risks regression model | Calibration plot (predicted risk against actual risk): less-well calibration (stroke and mortality) | C-statistic=0.6881 (stroke) | No |
Stevens et al. UKPDS 6624 | UK | MI case fatality and stroke case fatality | 5 (sex, HbA1c, SBP, previous stroke, white cell count for Stroke model) | Between 25 and 65 years | Both male and female | Stroke: 234/5102 | Median follow-up of 7 years | Stepwise selection algorithm | HL test: p=0.248 (Stroke model) | NR | No |
Tanaka et alJJ Risk Engine48 | Japan | CHD, stroke, non-cardiovascular mortality, overt nephropathy and progression of retinopathy | 11 (sex, age, HbA1c, years after diagnosis, BMI, non-HDL cholesterol, ACR, atrial fibrillation, current smoker and leisure-time physical activity) | 40–84 years | Both male and female | Stroke: 89/1748 | Median follow-up of 7.2 years | Cox regression model | HL test: p=0.12 (Stroke model) | C-statistic=0.636 (0.564 to 0. 708) (Stroke model) | No |
Palmer et al (IRS)23 | Scotland | Fatal or non-fatal stroke | 5 genotypes (IL-6 GG/GC, MCP- 1 GG, ICAM-1 EE, sel·E RR and MMP-3 5A5A) | Mean age 64.5±11.7 years | Both male and female | 108/2182 | Mean follow-up of 6.2±1.1 years | Cox regression model | NR | NR | No |
Kiadaliri et al 22 | Sweden | First and second events of: AMI, heart failure, non-acute ischaemic heart disease and stroke | 12 (age, TC/HDL, diabetes duration, HbAIc, BMI, SBP and diastolic BP, history of events before diagnosis, LDL cholesterol, albuminuria, smoking status, BMI and gender) | Male : mean age, 55.36±9.28 years; Female: mean age, 57.15±9.55 years |
Both male and female | 993/21 775 (first stroke); 314/21 775 (second stroke) | 82 232 person-years for first stroke and 4127 person-years for second stroke | Weibull proportional hazard model | HL χ2 statistic: 11.22 (p=0.19) (first stroke); 8.09 (p=0.43) (second stroke) | C-statistic=0.80 (0.78 to 0.82) (first stroke); C-statistic=0.74 (0.71 to 0.77) (second stroke) | No |
Li et al 49 | Taiwan | Ischaemic stroke | 14 (age, gender, smoking habit, duration of type 2 diabetes, blood pressure, HbA1c level, total cholesterol to HDL ratio, creatinine, fasting plasma glucose variation, arterial embolism and thrombosis, diabetes retinopathy, hypoglycaemia, antidiabetes medication use and cardiovascular medication) | 30–84 years | Both male and female | 2091 (derivation set), 1076 (validation set)/18 750 (derivation set), 9374 (validation set) | Mean follow-up of 8 years | Cox proportional hazard regression model | NR | AUROC=0.72 (3 years); AUROC=0.71 (5 years); AUROC=0.68 (8 years) | No |
Basu et al RECODe36 | USA and Canada | Microvascular: nephropathy, retinopathy, neuropathy; Cardiovascular: composite of atherosclerotic cardiovascular disease (first fatal or non-fatal MI or stroke), fatal or non-fatal MI, fatal or non-fatal stroke, congestive heart failure, or death from any cardiovascular cause | 14 (Age, sex, ethnicity, smoking, SBP, history of CVD, blood pressure-lowering drugs use, statin use, anticoagulants use, HbA1c, total cholesterol, HDL cholesterol, serum creatinine, urine ACR) | 40–79 years | Both male and female | 197 (stroke)/9635 | Median follow-up of 4.7 years | Cox proportional hazard models | Calibration slope=1.16, χ2=7.4, p value=0.38 (internal validation); calibration slope=0.99, χ2=8.2, p value=0.22 (external validation) | C-statistic for stroke=0.70 (0.66 to 0.74) (internal validation); C-statistic for stroke=0.67 (0.63 to 0.71) (external validation) | Yes |
ACR, albumin-to-creatinine ratio; AMI, acute myocardial infarction; AUROC, area under the receiver operating characteristic curve; BMI, body mass index; BP, blood pressure; CHD, coronary heart disease; CVD, cardiovascular disease; HDL, high-density lipoprotein; HL, Hosmer-Lemeshow; HbA1C, haemoglobin A1C; IRS, inflammatory risk score; JJ, The JDCS/J-EDIT; LDL, low-density lipoprotein; MI, myocardial infarction; NR, not reported; RECODe, Risk Equations for Complications of Type 2 Diabetes; SBP, systolic blood pressure; TC, total cholesterol; UKPDS, United Kingdom Prospective Diabetes Study.